阳极
材料科学
法拉第效率
电解质
锌
螯合作用
离子
化学工程
水溶液
扩散
无机化学
剥离(纤维)
图层(电子)
纳米技术
电极
化学
物理化学
冶金
有机化学
复合材料
物理
热力学
工程类
作者
Yuzhe Zhang,Rong Wang,Huaisheng Ao,Tao Ma,Xuekun Zhu,Xiaotan Zhang,Jian Rong,Ziyao Zhou,Zhongchao Bai,Shi Xue Dou,Nana Wang,Zhongyu Li
标识
DOI:10.1002/aenm.202404203
摘要
Abstract Aqueous Zn ion batteries hold great promise for next‐generation large‐scale energy storage systems due to their low cost, intrinsic safety, and environmental friendliness. However, the reversibility of Zn metal anodes is limited by severe side reactions and dendritic growth, caused by interfacial concentration gradients. To address this, a Zn 2+ ‐rich zinc phytate (ZP) chelate layer is introduced as artificial solid electrolyte interphase (SEI) that eliminates these concentration gradients through ions compensation. Theoretical calculations and experimental results demonstrate that the ZP layer, rich in Zn 2 ⁺ ions and exhibiting strong chelating ability to capture more Zn 2+ , enables rapid and dynamic ion replenishment at the interface, significantly improving Zn 2 ⁺ transport kinetics and ensuring a uniform Zn 2 ⁺ flux. Moreover, the strong chelation of PO₄ groups restricts the 2D diffusion of Zn 2 ⁺ ions, promoting the uniform Zn deposition. Additionally, the ZP layer repels anions and restricts water molecules migration at the Zn anode surface, fundamentally suppressing side reactions. As a result, the modified Zn anode exhibits stable Zn plating/stripping for ≈2400 h at 1 mA cm −2 and 1 mAh cm −2 , with an average Coulombic efficiency of 99.8%. Furthermore, the assembled ZP@Zn//VO 2 cell displays 87.5% capacity retention after 6000 cycles at the current density of 5 A g −1 .
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